Application of 16859-59-9, Because a catalyst decreases the height of the energy barrier, its presence increases the reaction rates of both the forward and the reverse reactions by the same amount.16859-59-9, Name is 3-Hydroxyisobenzofuran-1(3H)-one, molecular formula is C8H6O3. In a article£¬once mentioned of 16859-59-9
A palladium(II)-catalyzed cascade approach was established for the synthesis of indeno[1,2-c]isochromen-5(11H)-ones starting from 2-alkynyl tert-butyl benzoates bearing a pendant alpha,beta-unsaturated carbonyl moiety in high yields (up to 99%) under mild conditions. This strategy offered high atom and step economy by delivering isobutene as the only side product, and by generating two new bonds and two rings in a single synthetic operation. The mechanism of the cascade process was visualized comprising sequential intramolecular oxypalladation (6-endo-dig), intramolecular olefin insertion, and protonation steps. (Figure presented.).
A reaction mechanism is the microscopic path by which reactants are transformed into products. Each step is an elementary reaction. In my other articles, you can also check out more blogs about 16859-59-9
Reference£º
Benzofuran – Wikipedia,
Benzofuran | C8H1464O – PubChem